• Both normoxic and hypoxic preconditioned human amniotic mesenchymal stem cell exosomes significantly improved the proliferation of radiation-injured submandibular gland epithelial cells.
• Treatment with exosomes increased α-amylase secretion and aquaporin 5 mRNA expression in radiation-injured cells, indicating functional recovery.
• Hypoxic preconditioning of exosomes did not confer a statistically significant advantage over normoxic exosomes in repairing radiation damage.
• Exosomes derived from human amniotic mesenchymal stem cells may serve as a potential cell-free therapy for radiation-induced salivary gland injury.
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